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Thermal stress relaxation phenomenon through forming the interstitial region in CZ silicon pulled with rapid and slow cooling heat shields 热应力松弛现象通过形成间隙区域的CZ硅拉的快速和缓慢冷却隔热
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2022-08-01 DOI: 10.1016/j.pcrysgrow.2022.100579
Takao Abe
<div><p><span><span>This review article aims to clarify a mechanism of point defects formation in a CZ Si crystal through an experimental arrangement using the two kinds of heat shields with different slow-pulling periods. Point defects in a melt grown </span>silicon<span> crystal have been studied for a long time. The author and his co-researchers have reported about “Mechanism for generating interstitial atoms by thermal stress during silicon crystal growth” [in Progress in Crystal Growth and Characterization of Materials, </span></span><strong>66</strong><span> (2019) 36-46]. The experimental arrangement includes constant growing, changing pulling rate and finally detaching crystals from the melt. The two types of heat shields were used to change the cooling history of the grown crystals, for changing a temperature gradient at a bulk part in the grown crystal, </span><em>G</em><sub>b</sub>. In order to prove that the formation of an interstitial region or a boundary of vacancies (Vs)/interstitials (Is) in a silicon crystal is a phenomenon of relaxing thermal stress, the author explains that a <em>G</em><sub>b</sub> in a crystal forms thermal stress and causes some silicon atoms at lattice positions to move to the closest interstitial sites to relax the stress. The author defines a new term of metastable interstitial atom, I’, or I's as the plural of I’. The I’ coexists with the metastable vacancy V’ from where the I’ is displaced. The plural of V’ is defined to be V's. The author defines the above state to be a complex (I’+ V’), or (I ’+ V’)s as the plural of (I’+ V’), and explains that the (I’+ V’) s convert to Is and form the Is region. The (I’+ V’) is considered as the Frenkel pair-like complex.</p><p>The crystals were firstly pulled with a high pulling rate, and the pulling rate was consequently decreased to a slow one. Then the crystals were pulled with the slow constant pulling rate for different periods making different cooling processes. Finally, the grown crystals were detached from the melt and cooled rapidly. Characterization of defects, such as Vs, Is, and defect-free (D-F) regions were identified in X-ray topographs (XAOP(s)). Wafer lifetime mapping (WLTM(s)) allows confirming dislocation loop (DL) regions. The results show that the Is are generated depending on the pulling period of the slow pulling and the shapes of the heat shields. The Is and DL regions are formed in a region at temperatures near the melting point. The Is form an Is region through a defect-free (D-F) region, forming the Vs/Is boundary. When the thermal stress weakens, the DL region changes to the Is region; the Is region changes to the D-F region; and the D-F region changes to the Vs region. Temperature gradient distribution is induced toward various directions at different parts of the growing crystal depending on the different slow-pulling periods. The temperature gradient, <em>G</em><sub>b</sub>, includes a temperature gradient from the cooled region shaded
本文旨在通过两种不同慢拉周期的隔热层的实验布置,阐明czsi晶体中点缺陷的形成机制。熔体生长硅晶体中的点缺陷已经被研究了很长时间。作者和他的合作研究人员报道了“硅晶体生长过程中热应力产生间隙原子的机制”[在晶体生长和材料表征中的进展,66(2019)36-46]。实验安排包括恒定生长,改变拉速,最后从熔体中分离晶体。利用这两种类型的热屏蔽来改变生长晶体的冷却历史,从而改变生长晶体中块体部分的温度梯度。为了证明硅晶体中空位区或空位边界(Vs)/空位边界(Is)的形成是一种热应力松弛现象,作者解释了晶体中的一个Gb形成热应力,使晶格位置的一些硅原子移动到最近的空位位置以松弛应力。作者定义了一个亚稳态间隙原子的新名词I',或I's作为I'的复数形式。I '与亚稳空位V '共存,I '从那里被移开。V'的复数形式被定义为V's。作者将上述状态定义为复合体(I ' + V '),或者(I ' + V ')的复数形式(I ' + V '),并解释了(I ' + V ')转化为Is,形成Is区域。(I ' + V ')被认为是Frenkel对样复合体。首先以较高的拉拔速率对晶体进行拉拔,随后拉拔速率逐渐降低到较慢的拉拔速率。然后以缓慢恒定的拉拔速率对晶体进行不同周期的拉拔,形成不同的冷却过程。最后,生长的晶体从熔体中分离出来并迅速冷却。缺陷的表征,如v、i和无缺陷(D-F)区域在x射线地形图中被识别(XAOP(s))。晶圆寿命映射(WLTM(s))允许确认位错环(DL)区域。结果表明,慢拉过程的拉拔周期和隔热板的形状决定了热阻的产生。i区和DL区是在接近熔点的温度下形成的。通过无缺陷区(D-F)形成一个Is区,形成Vs/Is边界。当热应力减弱时,DL区变为Is区;Is区变为D-F区;D-F区变为v区。随着慢拉周期的不同,生长晶体不同部位的温度梯度分布也不同。温度梯度Gb包括从隔热罩遮蔽的冷却区域到生长界面的温度梯度和从长时间生长过程中冷却的上表面到生长界面的温度梯度。在熔点附近超过一定阈值的Gb形成热应力,产生Is使应力松弛。
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引用次数: 0
Growth, structure, electrical and optical properties of transition metal chalcogenide crystals synthesized by improved chemical vapor transport technique for semiconductor technologies 利用改进的半导体化学气相输运技术合成的过渡金属硫族化物晶体的生长、结构、电学和光学性质
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2022-08-01 DOI: 10.1016/j.pcrysgrow.2022.100578
Abhay Dasadia , Vidhi Bhavsar

Low dimensional structures, including bulk crystals, thin films, nanowires and nanotubes, have received remarkable attention due to their novel functionality and potential applications in various areas of optics, electronics, photonics, and sensing devices and photovoltaic field. Recently, remarkable progress and modification have been achieved in the synthesis process of crystalline material by vapor transport technique. In this review, we introduce an improved concept of the closed tube Chemical Vapor Transport (CVT) technique for the single crystal growth of ZrSTe, TiSTe and TiSeTe. A modified reverse temperature profile has reported the growth of ZrSTe, TiSTe and TiSeTe results show the good crystalline quality of synthesized materials. The single-crystal X-ray diffraction data reveals all three samples have trigonal unit cell structure with a space group of P31. The Semiconducting behavior of grown crystals of ZrSTe, TiSTe and TiSeTe was verified by two probe resistivity measurements, Hall Effect measurements and optical absorption at room temperature in the spectral range of 200 nm - 2200 nm. In this review, we highlight the recent progress in the transition of metal chalcogenides for their advanced application in solar energy conversion, thin-film electronics, optoelectronic devices and quantum communication devices. Moreover, different experimental challenges within the described growth technique are probed. Additionally, a survey was done for the possible enhancement of Transition Metal Chalcogenide (TMC) crystalline materials grown by the Chemical Vapor Transport technique based on various growth parameters.

低维结构,包括体晶体、薄膜、纳米线和纳米管,由于其新颖的功能和在光学、电子、光子学、传感器件和光伏领域的潜在应用而受到人们的广泛关注。近年来,利用气相输运技术合成结晶材料的工艺取得了显著的进展和改进。本文介绍了一种改进的封闭管化学气相传输(CVT)技术,用于ZrSTe、TiSTe和TiSeTe的单晶生长。修正后的反向温度谱报告了ZrSTe、TiSTe和TiSeTe的生长,结果表明合成材料具有良好的结晶质量。单晶x射线衍射数据显示,三种样品均具有三角形单晶结构,空间群为P31。在200 nm ~ 2200 nm的光谱范围内,通过两次探针电阻率测量、霍尔效应测量和室温光吸收,验证了ZrSTe、TiSTe和TiSeTe生长晶体的半导体行为。本文综述了近年来金属硫族化合物在太阳能转换、薄膜电子、光电子器件和量子通信器件等方面的应用进展。此外,本文还探讨了所述生长技术中的不同实验挑战。此外,基于不同的生长参数,探讨了化学气相输运技术生长过渡金属硫族化物(TMC)晶体材料的增强可能性。
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引用次数: 4
On the Vitality of the Classical Theory of Crystal Nucleation; Crystal Nucleation in Pure Own Melt; Atmospheric Ice and Snow; Ice in Frozen Foods 论经典晶体成核理论的生命力纯自身熔体结晶成核大气冰雪;冷冻食品中的冰
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2022-05-01 DOI: 10.1016/j.pcrysgrow.2022.100567
Christo N. Nanev
<div><p><span>The main reason for the longevity of the Classical Nucleation Theory (CNT) is its firm thermodynamic basis; reviewing the discussion about the molecular-scale mechanism of crystal nucleation from solutions, and especially the mechanism of protein crystal nucleation, we note that the diverse nucleation pathways across the metastable phase cannot contradict the thermodynamic conclusions of the CNT. In this review paper, revisiting the basic postulates of CNT, we argue that not only the energy barrier for crystal nucleation but the entire dependence of Gibbs’ thermodynamic potential on the crystal size is worth interpreting. In doing so, two supplementations to CNT have been elaborated. The first one concerns the theoretical method employing Equilibration between the Bond energy (i.e., the intra-crystalline cohesive energy which maintains the integrity of a crystalline cluster), and the surface Destructive Energy (tending to tear-up the crystal) - abbreviated EBDE. Second, we show that the dependence of the Gibbs’ thermodynamic potential on the crystal size determines not only the birth, but also the initial growth (or dissolution during Ostwald ripening) of the just born nuclei of the new phase; this is predicted in the negative branch of the said dependence. Initially, EBDE was used for explaining crystal nucleation from solutions, but most recently, this method was redefined for considering crystal nucleation in melts. The purposively redefined EBDE was applied for considering ice nucleation, which is an important case of spontaneous melt crystallization in nature - the quantitative consideration of the ice crystal nucleation is needed for better understanding of atmospheric processes, such as snowfall, white frost, sleet, hail, and ice fog. By focusing on the action of ice nucleating particles (INPs), which engender heterogeneous nucleation of ice, the snowfall is elucidated in a new way - ice nucleation in the atmosphere is considered as a two-step process, the first one being vapor </span>condensation in liquid droplets, and the second one - water freezing. Also, ice nucleation in frozen foods is re-considered applying EBDE. (It is known that freezing ensures a high-quality product and long shelf life of a wide range of food products, such as fish, meat, vegetables, tropical fruits, coffee, flavor essence, etc.) And because numbers and sizes of ice crystals are decisive for the degree of deterioration of food quality due to freezing, the mean sizes of the ice crystals (which depend on their number) are considered in a quantitative manner. Also, another consideration concerns ice crystal nucleation and growth occurring by freeze concentration of liquid foods. Although aimed at reviewing fundamental aspects of crystal nucleation, it is to be hoped that some results of the considerations in this paper may also be beneficial for practical applications; suggestions in this respect are mentioned throughout the paper. For instance, the
经典成核理论(CNT)经久不衰的主要原因是其坚实的热力学基础;回顾有关溶液晶体成核的分子尺度机制,特别是蛋白质晶体成核机制的讨论,我们注意到亚稳相上不同的成核途径不能与碳纳米管的热力学结论相矛盾。在本文中,我们回顾了碳纳米管的基本假设,我们认为不仅晶体成核的能量势垒,而且Gibbs热力学势对晶体尺寸的整个依赖关系都值得解释。在这样做的过程中,拟定了对CNT的两个补充。第一个是关于利用键能(即维持晶簇完整性的晶内内聚能)和表面破坏能(倾向于撕裂晶体)之间的平衡的理论方法-简称EBDE。其次,我们证明了吉布斯热力学势对晶体尺寸的依赖关系不仅决定了新相的诞生,而且决定了新相刚诞生的核的初始生长(或奥斯特瓦尔德成熟期间的溶解);这是在上述依赖性的负分支中预测的。最初,EBDE用于解释溶液中的结晶成核,但最近,该方法被重新定义为考虑熔体中的结晶成核。有目的地重新定义的EBDE用于考虑冰的成核,这是自然界中熔体自发结晶的一个重要案例-需要定量考虑冰晶成核,以便更好地理解大气过程,如降雪,白霜,雨雪,冰雹和冰雾。通过关注冰成核粒子(INPs)对冰非均相成核的作用,从一个新的角度来解释降雪过程——将大气中的冰成核看作是一个两步过程,第一步是液滴中的水蒸气凝结,第二步是水的冻结。此外,应用EBDE重新考虑冷冻食品中的冰核。(众所周知,冷冻可以确保各种食品的高质量产品和长保质期,如鱼、肉、蔬菜、热带水果、咖啡、香精等)并且由于冰晶的数量和大小对食品质量因冷冻而恶化的程度具有决定性作用,因此以定量的方式考虑冰晶的平均大小(取决于它们的数量)。此外,另一个需要考虑的问题是液态食品在冷冻浓缩过程中发生的冰晶成核和生长。虽然目的是回顾晶体成核的基本方面,但希望本文考虑的一些结果也可能对实际应用有益;这方面的建议贯穿全文。例如,直接比较纯水和冷冻食品中的冰晶成核,可以优化食品的动态冷冻步骤等。回顾以一小段介绍碳纳米管的优点和缺点结束。
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引用次数: 4
The formation of crystalline minerals and their role in the origin of life on Earth 结晶矿物的形成及其在地球生命起源中的作用
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2022-02-01 DOI: 10.1016/j.pcrysgrow.2022.100558
Cesia D. Pérez-Aguilar, Mayra Cuéllar-Cruz

As known currently, in the formation of the Earth, minerals have played a pivotal role going from the formation of the hydrosphere, the lithosphere, and all Earth components until the origin, evolution, and maintenance of life. The first signs of magnetism are found in komatiites. In the origin of life, minerals were responsible for concentrating, aligning, and acting as templates and catalyzers, allowing for the formation of bonds among the first biomolecules to form polymers, which eventually became assembled to give rise to the pioneer organism in the Precambrian. Besides, minerals allowed the DNA to be the information storing molecule, even though it was not the first biomolecule. Another function of minerals was to protect the organic complexes against ultraviolet radiation and hydrolysis, a fundamental action to preserve life in the Precambrian where high UV radiation prevailed. Minerals not only favored the origin of life but also became part of the organisms that inhabit the Earth, including species of the five kingdoms, comprising from microorganisms to higher organisms. How minerals participated in the origin of life still has unresolved questions, for which to understand the minerals’ participation since the formation of the Earth until becoming part of the structure of organisms from the five kingdoms, we reviewed the following topics, which will contribute to the understanding of the implication of minerals in the origin of our planet and life on it: i) the synthesis of the chemical elements from which the first mineral were obtained in the Earth, ii) the factor that favored the formation of minerals in the Earth, iii) the implication of minerals as the basis for the synthesis of the first biomolecule and, eventually, the pioneer organism, as well as the biomineralization mechanism that has been proposed to account for the mineral part contained in the structure of the organisms from the different kingdoms, and iv) the models that allow emulating the mechanisms by which minerals participated in the synthesis of the first biomolecule; in this way, for example, the Precambrian microfossils are so simple morphologically (spheres, subspheres, and hemispheres) that they can easily be imitated by hollow mineral growths, known as biomorphs. Although these can interfere with the study of actual microfossils, they remain as key points for the study of the origin of life.

众所周知,在地球的形成过程中,从水圈、岩石圈和地球的所有组成部分的形成,到生命的起源、进化和维持,矿物质都起着举足轻重的作用。最初的磁性迹象是在科马陨石中发现的。在生命的起源中,矿物质负责浓缩、排列,并充当模板和催化剂,允许在第一批生物分子之间形成键,形成聚合物,这些聚合物最终聚集在一起,产生了前寒武纪的先锋生物。此外,尽管DNA不是第一个生物分子,但矿物质使它成为信息存储分子。矿物质的另一个功能是保护有机复合物免受紫外线辐射和水解,这是在高紫外线辐射盛行的前寒武纪保存生命的基本作用。矿物不仅有利于生命的起源,而且也成为了居住在地球上的生物的一部分,包括五大王国的物种,从微生物到高等生物。矿物是如何参与生命起源的至今仍是一个未解决的问题,为了理解矿物从地球形成到成为五界生物结构的一部分的参与,我们回顾了以下几个主题,这将有助于理解矿物在地球起源和生命起源中的含义:1)在地球上获得第一个矿物的化学元素的合成,2)有利于地球矿物形成的因素,3)矿物作为合成第一个生物分子并最终形成先驱生物的基础的含义,以及为解释来自不同王国的生物结构中所含矿物部分而提出的生物矿化机制,iv)模拟矿物参与第一个生物分子合成的机制的模型;通过这种方式,例如,前寒武纪微化石在形态上是如此简单(球体、亚球体和半球),以至于它们很容易被中空的矿物生长(称为生物形态)所模仿。尽管这些可能会干扰对实际微化石的研究,但它们仍然是研究生命起源的关键点。
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引用次数: 7
A short overview on practical techniques for protein crystallization and a new approach using low intensity electromagnetic fields 简要介绍了蛋白质结晶的实用技术和利用低强度电磁场的新方法
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2022-02-01 DOI: 10.1016/j.pcrysgrow.2022.100559
Camila Campos-Escamilla , Luis A. Gonzalez-Rámirez , Fermín Otálora , José Antonio Gavira , Abel Moreno

This contribution deals with a practical overview of some popular and sophisticated crystallization methods that help increase the success rate of a crystallization project and introduces a newly developed method involving low intensity electromagnetic fields. Aiming to suggest a methodology to follow, the present contribution is divided into two main parts in a logical order to get the best crystals for high resolution X-ray crystallographic analysis. The first part starts with a short review of the chemical and physical fundamentals of each crystallization method through different strategies based on physicochemical approaches. Then, practical non-conventional techniques for protein crystallization are presented, not only for growing protein crystals, but also for controlling the size and number of crystals. These include crystal growth in gels, counter-diffusion, seeding, and macromolecular imprinted polymers (MIPs). The second part shows the effects of coupling low intensity electric fields (in the scale of units of  μAmperes) with weak magnetic fields (in the scale of milli Tesla) applied to protein crystallization. This approach consists of a novel experimental set up, which was used to study the influence of the coupled fields on the crystallization of lysozyme in solution and in gel media. This new approach is based on the classical theories of transport phenomena and offers a more accessible strategy to obtain suitable crystals for X-ray characterization or Neutron diffraction investigations.

本文介绍了一些常用的复杂结晶方法的实际概况,这些方法有助于提高结晶项目的成功率,并介绍了一种涉及低强度电磁场的新开发方法。为了提出一种可遵循的方法,本文按照逻辑顺序分为两个主要部分,以获得用于高分辨率x射线晶体学分析的最佳晶体。第一部分通过基于物理化学方法的不同策略,简要回顾了每种结晶方法的化学和物理基础。然后,提出了实用的非常规蛋白质结晶技术,不仅用于生长蛋白质晶体,而且用于控制晶体的大小和数量。这些包括凝胶晶体生长,反扩散,播种和高分子印迹聚合物(MIPs)。第二部分展示了低强度电场(以μ安培为单位)与弱磁场(以毫特斯拉为单位)耦合对蛋白质结晶的影响。该方法包括一个新的实验装置,用于研究耦合场对溶液和凝胶介质中溶菌酶结晶的影响。这种新方法基于经典输运现象理论,为获得适合x射线表征或中子衍射研究的晶体提供了一种更容易获得的策略。
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引用次数: 3
In-situ optical microscopy observation of elementary steps on ice crystals grown in vapor and their growth kinetics 原位光学显微镜观察冰晶在蒸汽中生长的基本步骤及其生长动力学
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2021-11-01 DOI: 10.1016/j.pcrysgrow.2021.100550
Gen Sazaki , Masahiro Inomata , Harutoshi Asakawa , Etsuro Yokoyama , Shunichi Nakatsubo , Ken-ichiro Murata , Ken Nagashima , Yoshinori Furukawa

Ice is one of the most abundant materials on the earth's surface, and its growth governs various natural phenomena. Hence, the molecular-level understanding of ice crystal surfaces is crucially important. However, it is generally acknowledged that the molecular-level observation of ice crystal surfaces by ordinary microscopy techniques, such as atomic force microscopy and scanning electron microscopy, is very difficult at temperatures near the melting point (0 °C). To overcome such difficulties, we have developed laser confocal microscopy combined with differential interference contrast microscopy (LCM-DIM). We proved that LCM-DIM can visualize individual elementary steps (0.37 nm in thickness) on a basal face by observing two-dimensional nucleation growth. Then we found by LCM-DIM that spiral steps on a basal face exhibit a double-spiral pattern, which can be expected from ice's crystallographic structure. In addition, we revealed that temperature dependence of growth kinetics of elementary spiral steps on a basal face exhibits complicated behaviors, which show the presence of unknown phenomena in the growth kinetics. Furthermore, we proved that surface diffusion of water admolecules on a basal face plays a crucially important role in the lateral growth of elementary steps when the distance between adjacent spiral steps is smaller than 15 µm. These findings will provide a clue for unlocking growth kinetics of ice crystals. In addition, through the use of LCM-DIM much progress has been made in studies on the surface melting of ice and the interaction between ice and atmospheric gasses.

冰是地球表面最丰富的物质之一,它的生长支配着各种自然现象。因此,在分子水平上理解冰晶表面是至关重要的。然而,人们普遍认为,在接近熔点(0°C)的温度下,用原子力显微镜和扫描电子显微镜等普通显微镜技术对冰晶表面进行分子水平的观察是非常困难的。为了克服这些困难,我们开发了激光共聚焦显微镜结合差干涉对比显微镜(LCM-DIM)。通过观察二维成核生长,我们证明LCM-DIM可以在基面上可视化单个基本步骤(厚度为0.37 nm)。通过LCM-DIM分析,我们发现基面上的螺旋台阶呈双螺旋状,这可以从冰的晶体结构中得到预测。此外,我们发现基面上基本螺旋台阶的生长动力学的温度依赖表现出复杂的行为,这表明生长动力学中存在未知现象。此外,我们证明了当相邻螺旋台阶之间的距离小于15µm时,水分子在基面上的表面扩散对基本台阶的横向生长起着至关重要的作用。这些发现将为解开冰晶的生长动力学提供线索。此外,通过使用LCM-DIM,在冰的表面融化和冰与大气气体相互作用的研究方面取得了很大进展。
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引用次数: 2
CdTe-based crystals with Mg, Se, or Mn as materials for X and gamma ray detectors: Selected physical properties 以镁、硒或锰为材料的碲基晶体用于X射线和伽马射线探测器:选定的物理性质
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2021-11-01 DOI: 10.1016/j.pcrysgrow.2021.100543
Andrzej Mycielski , Aneta Wardak , Dominika Kochanowska , Marta Witkowska-Baran , Michał Szot , Rafał Jakieła , Jarosław Z. Domagała , Leszek Kowalczyk , Michał Kochański , Gabriela Janusz , Marcin Dopierała , Adam Marciniak , Barbara Witkowska , Bartłomiej S. Witkowski , Anna Reszka , Andrei Avdonin , Elżbieta Łusakowska , Witold Chromiński , Małgorzata Lewandowska , Małgorzata Górska

In recent years, a series of investigations has been devoted to a possibility of using crystals based on CdTe with addition of magnesium (Mg), selenium (Se), or manganese (Mn) for X and gamma radiation detectors. In the literature there are contradictory data with respect to the segregation of Mg in (Cd,Mg)Te and Se in Cd(Te,Se) and to the possibility of obtaining materials with a homogeneous composition without grains and twins.

We have wide technological possibilities of preparing crystals and investigating some of their properties. Thus, we performed crystallizations of (Cd,Mg)Te, Cd(Te,Se), (Cd,Mn)(Te,Se), and (Cd,Mn)Te compounds. The aim of our studies was to check whether any of the investigated materials may be easily obtained by the Low Pressure Bridgman (LPB) method in the form of large, homogeneous, high resistivity single crystals with as few as possible twins, subgrains, and tellurium inclusions.

The crystallization processes were performed by using the LPB method. The elements used: Cd, Te, Mn, Mg, and Se were of the highest purity available at that time. In order to obtain reliable conclusions the crystallization processes were carried out under identical technological conditions. The details of our technological method and the results of the investigation of physical properties of the samples are presented below.

近年来,人们进行了一系列的研究,以探索在CdTe基础上添加镁(Mg)、硒(Se)或锰(Mn)的晶体用于X和伽马辐射探测器的可能性。在文献中,关于(Cd,Mg)Te中Mg的偏析和Cd(Te,Se)中Se的偏析以及获得没有晶粒和孪晶的均匀成分的材料的可能性,存在矛盾的数据。我们有广泛的技术可能性来制备晶体和研究它们的一些性质。因此,我们进行了(Cd,Mg)Te, Cd(Te,Se), (Cd,Mn)(Te,Se)和(Cd,Mn)Te化合物的结晶。我们研究的目的是检查是否有任何被研究的材料可以很容易地通过低压桥曼(LPB)方法以大的,均匀的,高电阻率的单晶形式获得,尽可能少的孪晶,亚晶和碲包裹体。结晶过程采用LPB法进行。所使用的元素:Cd, Te, Mn, Mg和Se是当时可用的最高纯度。为了得到可靠的结论,在相同的工艺条件下进行了结晶过程。我们的技术方法的细节和样品的物理性质的调查结果如下。
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引用次数: 9
Semi-wet growth and characterization of multi-functional nano-engineered mixed metal oxides for industrial application 工业用途多功能纳米工程混合金属氧化物的半湿生长和表征
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2021-11-01 DOI: 10.1016/j.pcrysgrow.2021.100542
Laxman Singh , Ravikant Sharma , Narayan Singh , Atendra Kumar , Dev K Mahato , Youngil Lee , Mikhael Bechelany , KD Mandal

This review paper covers the low temperature wet growth of nano-engineered particles of ZnO-based mixed metal oxides, their growth mechanism, and characterization using X-ray diffraction, SEM, TEM and IR, UV–visible, and XPS spectral techniques. Main focus of this article is centered on low temperature semi-wet methods of synthesis that are suitable for large scale production of zinc oxide-based systems mixed with iron oxide, copper oxide, nickel oxide and cobalt oxide. These mixed metal oxides have broad industrial applications as catalyst, semiconductors, adsorbents, superconductors, electro-ceramics, and antifungal agents in addition to extensive applications in medicines. This paper discusses the low-cost and environment friendly synthesis of these mixed metal oxides, measurement of properties and applicability of these materials systems.

本文综述了zno基混合金属氧化物纳米工程颗粒的低温湿生长及其生长机理,并利用x射线衍射、扫描电镜、透射电镜、红外光谱、紫外可见和XPS光谱技术对其进行了表征。本文主要研究了适用于大规模生产氧化锌、氧化铁、氧化铜、氧化镍和氧化钴混合体系的低温半湿合成方法。这些混合金属氧化物具有广泛的工业应用,如催化剂、半导体、吸附剂、超导体、电陶瓷和抗真菌剂,以及广泛的医药应用。本文讨论了这些混合金属氧化物的低成本和环境友好的合成方法,以及这些材料体系的性能测试和适用性。
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引用次数: 3
Growth, characterization and performance of bulk and nanoengineered molybdenum oxides for electrochemical energy storage and conversion 用于电化学储能和转换的大块和纳米氧化钼的生长、表征和性能
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2021-08-01 DOI: 10.1016/j.pcrysgrow.2021.100533
C.V. Ramana , A. Mauger , C.M. Julien
<div><p>Molybdenum oxides (MoO<sub>y</sub>) exhibit quite interesting structural, chemical, electrical, optical and electrochemical properties, which are often dependent on the synthetic procedures and fabrication conditions. The MoO<sub>y</sub> materiails are promising in numerous current and emerging technological applications, which include nanoelectronics, optoelectronics, energy storage and micromechanics. However, fundamental understanding of the crystal structure and engineering the phase and microstructure is the key to achieving the desired properties and performance in all of these applications. Therefore, in this review, an attempt made to provide a comprehensive review by considering the illustrative examples to highlight the fundamental scientific issues, challenges, and opportunities as related to various Mo-oxides applicable to electrochemical energy applications. In the course of development of lithium batteries delivering high-power and high-energy density for powering electric vehicles, here in this paper, we examine the performances of Mo-oxides, which are candidates as electrodes materials primarily for lithium-ion batteries (LIBs), while some aspects considered in sodium-ion batteries (SIBs) or electrochemical supercapacitors (ECs). Due to the wide range of oxidation states (from +6 to +2) they are promising as both positive (cathode) and negative (anode) electrodes of electrochemical cells. Based on their specific structural, chemical, electrical, and optical properties, which are dependent on the growth conditions and the fabrication technique, this review highlights the progress made in improving and understanding the electrochemical performance of MoO<sub>y</sub> compounds. Various materials (2.0 ≤ <em>y</em> ≤ 3.0) including anhydrous, hydrates, nanorods, nanobelts, composites and thin films of MoO<sub>y</sub> are considered. Due to their higher oxidation states, MoO<sub>y</sub> compounds undergo reversible topotactic lithium intercalation reactions; however, electrochemical features appear strongly dependent on the crystal quality and structural arrangement in the host lattice. Using <em>in-situ</em> and <em>ex-situ</em> X-ray diffraction and Raman spectroscopic data, structural characteristics of various MoO<sub>y</sub> are discussed. While the reasons for first-cycle irreversible capacity losses identified and discussed elaborately, the approaches adopted for enhanced performance and/or improvements also summarized. Several sub-stoichiometric MoO<sub>y</sub> positive electrodes exhibit excellent cycle life (up to 300 cycles) with high initial coulombic efficiency (80–90%) and large reversible capacity (>300 mAh g<sup>−1</sup>). Molybdenum oxides also categorized as one of the conversion-type transition-metal oxides and applied as negative electrodes for LIBs and SIBs with a specific capacity approaching 1000 mAh g<sup>−1</sup>. In addition to the discussion of the key aspects of crystal growth, characterization, an
钼氧化物(moy)表现出非常有趣的结构、化学、电学、光学和电化学性质,这些性质往往取决于合成方法和制造条件。MoOy材料在包括纳米电子学、光电子学、能量存储和微观力学在内的许多当前和新兴技术应用中都有前景。然而,对晶体结构的基本理解以及对相和微观结构的工程设计是在所有这些应用中实现所需性能和性能的关键。因此,在这篇综述中,试图通过举例来提供一个全面的综述,以突出与各种氧化钼应用于电化学能源相关的基本科学问题、挑战和机遇。在为电动汽车提供高功率和高能量密度的锂电池的开发过程中,在本文中,我们研究了mo -氧化物的性能,它主要是锂离子电池(lib)的候选电极材料,而钠离子电池(sib)或电化学超级电容器(ECs)则考虑了一些方面。由于氧化态范围广(从+6到+2),它们有希望作为电化学电池的正(阴极)和负(阳极)电极。基于其特定的结构,化学,电学和光学性质,这些性质取决于生长条件和制造技术,本文综述了在改善和理解MoOy化合物电化学性能方面取得的进展。考虑了各种材料(2.0≤y≤3.0),包括无水、水合物、纳米棒、纳米带、复合材料和moy薄膜。由于其较高的氧化态,MoOy化合物发生可逆的拓扑锂嵌入反应;然而,电化学特性似乎强烈依赖于晶体质量和主晶格中的结构排列。利用原位和非原位x射线衍射和拉曼光谱数据,讨论了各种moy的结构特征。在详细确定和讨论了第一周期不可逆容量损失的原因的同时,还总结了为提高性能和/或改进所采取的方法。几种亚化学计量moy正极具有优异的循环寿命(高达300次循环),具有高初始库仑效率(80-90%)和大可逆容量(>300 mAh g - 1)。钼氧化物也被归类为转换型过渡金属氧化物之一,应用于lib和sib的负极,比容量接近1000 mAh g−1。除了讨论晶体生长、表征和结构-性能关系的关键方面外,还提出并讨论了设计氧化钼材料以提高结构稳定性和电化学性能的未来前景。
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引用次数: 10
Progress in-situ synthesis of graphitic carbon nanoparticles with physical vapour deposition 物理气相沉积原位合成石墨碳纳米颗粒的研究进展
IF 5.1 2区 材料科学 Q1 CRYSTALLOGRAPHY Pub Date : 2021-08-01 DOI: 10.1016/j.pcrysgrow.2021.100534
Abdul Wasy Zia , Martin Birkett , Mohsin Ali Badshah , Munawar Iqbal

Graphitic carbon nanoparticles are in high demand for sensing, health care, and manufacturing industries. Physical vapour deposition (PVD) methods are advantageous for in-situ synthesis of graphitic carbon particles due to their ability to produce large area distributions. However, the carbon particles can agglomerate, irrespective of the PVD method, and form coagulated structures while growing inside the vacuum chamber. The random shapes and sizes of these particles lead to non-uniform properties and characteristics, hence making them less attractive for numerous industrial applications, such as energy storage batteries and structural health monitoring. Therefore, the in-situ synthesis of isolated carbon particles produced in a single-step PVD process having control over size, shape, and large area distributions has remained inspiring for the past 30 years. This article gives an overview of characteristics, applications, industrial impact, and global revenue of graphite particles. A critical review on in-situ growth of graphitic carbon particles with different PVD methods is described with selected examples. A comprehensive summary compares the capability of different PVD techniques and corresponding carbon resources to produce graphitic particles with numerous sizes and shapes. Analysing the outputs of various PVD methods, a generalised four-stage model is explained to understand the in-situ growth of graphitic carbon particles, which start from seedings and grow as particles, clusters, and granular structures. It is concluded that the isolated carbon particles can be produced with specific size, shape, and distributions irrespective of the PVD method employed, by maintaining precise control over combinations of deposition system properties and process parameters.

石墨碳纳米颗粒在传感、医疗保健和制造业中有很高的需求。物理气相沉积(PVD)方法有利于原位合成石墨碳颗粒,因为它们能够产生大面积分布。然而,无论PVD方法如何,碳颗粒都可以凝聚,并在真空室中生长时形成凝固结构。这些颗粒的随机形状和大小导致其性质和特性不均匀,因此对储能电池和结构健康监测等许多工业应用不太有吸引力。因此,在过去的30年里,原位合成在单步PVD工艺中产生的分离碳颗粒具有控制尺寸,形状和大面积分布的特性。本文概述了石墨颗粒的特点、应用、工业影响和全球收入。对不同PVD法原位生长石墨碳颗粒的研究进展进行了综述,并列举了一些实例。综合总结比较了不同PVD技术和相应的碳资源生产各种尺寸和形状的石墨颗粒的能力。分析了各种PVD方法的输出,解释了一个广义的四阶段模型,以理解石墨碳颗粒的原位生长,从种子开始,生长为颗粒、簇和颗粒结构。结果表明,通过对沉积系统性能和工艺参数的精确控制,无论采用何种PVD方法,都可以获得具有特定尺寸、形状和分布的分离碳颗粒。
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引用次数: 8
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Progress in Crystal Growth and Characterization of Materials
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